Canonical Allele Identifier: CA2059747651

Gene: C12orf42

Linked Data

• dbSNP Id: rs10861032

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.103518728T>G , CM000674.2:g.103518728T>G	GRCh38
NC_000012.11:g.103912506T>G , CM000674.1:g.103912506T>G	GRCh37
NC_000012.10:g.102436636T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011538291.1:c.36+5384A>C	XP_011536593.1:n.36+5384A>C
XM_011538294.1:c.36+5384A>C	XP_011536596.1:n.36+5384A>C
XM_011538306.1:c.36+5384A>C	XP_011536608.1:n.36+5384A>C
XM_011538307.1:c.36+5384A>C	XP_011536609.1:n.36+5384A>C
XM_011538308.1:c.36+5384A>C	XP_011536610.1:n.36+5384A>C
XM_011538309.1:c.36+5384A>C	XP_011536611.1:n.36+5384A>C
XM_011538310.1:c.36+5384A>C	XP_011536612.1:n.36+5384A>C
XM_011538311.1:c.36+5384A>C	XP_011536613.1:n.36+5384A>C
XM_011538312.1:c.36+5384A>C	XP_011536614.1:n.36+5384A>C
XM_011538313.1:c.36+5384A>C	XP_011536615.1:n.36+5384A>C
XM_011538314.1:c.36+5384A>C	XP_011536616.1:n.36+5384A>C
XM_011538315.1:c.36+5384A>C	XP_011536617.1:n.36+5384A>C
XM_011538316.1:c.36+5384A>C	XP_011536618.1:n.36+5384A>C
XM_011538317.1:c.36+5384A>C	XP_011536619.1:n.36+5384A>C
XR_944538.1:n.125+5384A>C
XR_944539.1:n.125+5384A>C
XR_944540.1:n.122+5384A>C
XR_944541.1:n.122+5384A>C
XR_944542.1:n.122+5384A>C
XR_944543.1:n.122+5384A>C
XR_944544.1:n.122+5384A>C
XM_011538294.2:c.36+5384A>C	XP_011536596.1:n.36+5384A>C
XM_011538308.2:c.36+5384A>C	XP_011536610.1:n.36+5384A>C
XM_011538312.2:c.36+5384A>C	XP_011536614.1:n.36+5384A>C
XM_011538315.2:c.36+5384A>C	XP_011536617.1:n.36+5384A>C
XM_017019281.1:c.36+5384A>C	XP_016874770.1:n.36+5384A>C
XR_001748690.1:n.130+5384A>C
XR_001748691.1:n.127+5384A>C
XR_001748692.1:n.126+5384A>C
XR_001748693.1:n.126+5384A>C
XR_001748694.1:n.126+5384A>C